IP Library Granted Patent US 9,642,941
Granted Patent B2
US 9,642,941 · App. 14/305,424 · Granted May 9, 2017

Implantable modular hydrogel for salivary gland restoration

Inventors: Robert L. Witt (Kennett Square, PA); Xinqiao Jia (Newark, DE); Swati Pradham Bhatt (Newark, DE); Mary C. Farach-Carson (Houston, TX); Daniel A. Harrington (Houston, TX)
Assignee: WILLIAM MARSH RICE UNIVERSITY
A61L27/54A61L27/26A61L27/38A61L27/3813A61L27/48A61L27/52A61L2430/34
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Quick Facts
Patent No.
US 9,642,941
App. No.
14/305,424
Granted
May 9, 2017
Kind
B2
Abstract

Implantable modular hydrogels to aid in salivary gland restoration and associated methods are provided. In one embodiment, the present disclosure provides for a hydrogel network comprising: a hyaluronic acid macromer crosslinked with a multiblock copolymer.

Claims (26)

1. A hydrogel network comprising: a hyaluronic acid macromer crosslinked with a crosslinker, wherein the crosslinker is a multiblock copolymer, wherein the multiblock copolymer comprises an alternating copolymer of poly(ethylene glycol) (PEG) and a peptide epitope of perlecan, or an alternating copolymer of poly(acrylic acid) and a hydrophobic peptide.

2. The hydrogel network of claim 1 , wherein the multiblock copolymer comprises a multiblock copolymer of perlecan domain IV (P1nDIV) peptide alternating with PEG.

3. The hydrogel network of claim 1 , wherein the multiblock copolymer comprises a multiblock copolymer of poly(acrylic acid) alternating with a hydrophobic peptide of sequence (VPGVG) 2 .

4. The hydrogel network of claim 1 wherein the hydrogel network is biocompatible.

5. A kit comprising a hyaluronic acid macromer and a crosslinker, wherein the crosslinker is a multiblock copolymer, wherein the multiblock copolymer comprises an alternating copolymer of poly(ethylene glycol) and a peptide epitope of perlecan, or an alternating copolymer of poly(acrylic acid) and a hydrophobic peptide.

6. The kit of claim 5 wherein the hyaluronic acid macromer comprises an unsaturated double bond.

7. The kit of claim 5 wherein the hyaluronic acid macromer comprises an acrylate.

8. The kit of claim 5 further comprising hyaluronic acid hydrogel particles.

9. The kit of claim 8 wherein the hyaluronic acid hydrogel particles further comprise a growth factor.

10. The kit of claim 8 wherein the hyaluronic acid hydrogel particles are angiogenic.

11. A method of forming a hydrogel network comprising: providing a hyaluronic acid macromer; providing a crosslinker, wherein the crosslinker is a multiblock copolymer comprising an alternating copolymer of PEG and a peptide epitope of perlecan, or an alternating copolymer of poly(acrylic acid) and a hydrophobic peptide, and crosslinking the hyaluronic acid macromer with the crosslinker to form the hydrogel network.

12. The method of claim 11 , wherein the multiblock copolymer comprises a multiblock copolymer of P1nDIV peptide alternating with PEG.

13. The method of claim 11 , wherein the multiblock copolymer comprises a multiblock copolymer of poly(acrylic acid) alternating with a hydrophobic peptide of sequence (VPGVG)2.

14. The method of claim 11 further comprising encapsulating cells within the hydrogel network.

15. The method of claim 11 further comprising encapsulating hyaluronic acid hydrogel particles within the hydrogel network.

16. The method of claim 11 wherein two or more hydrogel networks are combined to form a secondary hydrogel network.

17. The method of claim 16 wherein the secondary hydrogel network is a 3D construct.

18. A method of constructing a biomimetic matrix comprising:

providing a hyaluronic acid hydrogel network comprising a hyaluronic acid macromer crosslinked with a crosslinker, wherein the crosslinker is a multiblock copolymer comprising an alternating copolymer of poly(ethylene glycol) (PEG) and a peptide epitope of perlecan, or an alternating copolymer of poly(acrylic acid) and a hydrophobic peptide;

providing hyaluronic acid hydrogel particles;

providing salivary cells; and

co-encapsulating the hyaluronic acid hydrogel particles and the salivary cells within the hyaluronic acid hydrogel network to form cell-laden microgel modules.

19. The method of claim 18 , further comprising: combining multiple cell-laden microgel modules into a secondary hyaluronic acid network to yield a 3D network.

20. The method of claim 18 wherein the cells are treated with at least one of a β-adrenergic agonist, a M3 muscarinic agonist, and combinations thereof.

21. A composition comprising: a hyaluronic acid macromer; a crosslinker comprising a multiblock copolymer comprising a copolymer of P1nDIV peptide alternating with PEG; and hyaluronic acid hydrogel particles.

22. The composition of claim 21 further comprising cells.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jun 9, 2016
From: RICE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 038854/0086 →
Continuity (3)
Continuation PCTUS2012070173 · Dec 17, 2012
Provisional Application 61576721 · Dec 16, 2011
Related Publication 20140294960A1 · Oct 2, 2014